催化作用
光催化
格式化
石墨烯
氧化物
纤维素
材料科学
制氢
水解
甲酸甲酯
光化学
化学工程
无机化学
化学
纳米技术
有机化学
工程类
作者
Van‐Can Nguyen,Dipak B. Nimbalkar,Le D. Nam,Yuh‐Lang Lee,Hsisheng Teng
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2021-04-08
卷期号:11 (9): 4955-4967
被引量:104
标识
DOI:10.1021/acscatal.1c00217
摘要
The mechanism of photocatalytic biomass reforming for H2 production is far from fully understood. This study uses functionalized graphene dots with Pt-cocatalyst to reform cellulose in an alkaline solution under 1 sun illumination. Reforming of cellulose is initiated with the peeling of its constituent d-glucose units, which subsequently transform into deprotonated isosaccharinic acid (C6). Further degradation of C6 into molecules C5-C1 proceeds through successive alternation of C-eliminating hydrolysis and photocatalytic oxidation of C6 derivatives. The C6-C1 species are quantitatively identified using chromatography and mass spectroscopy. The end C-containing product is predominantly HCOO– rather than HCO3– (or CO2). The photocatalytic oxidation is accompanied by the photocatalytic reduction of water to produce H2. This reforming steadily produced H2 for 6 days with a negligible rate decay, accomplishing 35% of the theoretical ultimate value for the reforming of cellulose. This study elucidates the detailed mechanism in the photocatalytic reforming of cellulose.
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